chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4158110101158110102CT64GENIChomozygous137249414
4158110674158110674GTGTGTGT37GENIChomozygous136925444
4158110676158110676GTGTGT38GENIChomozygous136925445
4158110718158110719CT40GENIChomozygous137249415
4158111131158111132GA28GENIChomozygous137249416
4158111297158111298GA50GENIChomozygous137249417
4158111866158111867CT47GENICpossibly homozygous137249418
4158111878158111879CT47GENICpossibly homozygous137249419
4158112592158112593TC32GENIChomozygous137249420
4158113686158113687AG64GENIChomozygous137249421
4158115264158115265TC60GENIChomozygous137249422
4158110981158110982C40GENICpossibly homozygous403125319
4158110981158110982CT40GENICheterozygous403125320